No abstract available. Comment on - ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis. [Eur J Hum Genet. 2015] - Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. [Eur J Hum Genet. 2014]

Ceroni, F., Simpson, N.H., Francks, C., Baird, G., Conti-Ramsden, G., Clark, A., et al. (2015). Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'. EUROPEAN JOURNAL OF HUMAN GENETICS, 23(9), 1113-1115 [10.1038/ejhg.2014.275].

Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'

CERONI, FABIOLA;MAESTRINI, ELENA;BACCHELLI, ELENA;
2015

Abstract

No abstract available. Comment on - ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis. [Eur J Hum Genet. 2015] - Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. [Eur J Hum Genet. 2014]
2015
Ceroni, F., Simpson, N.H., Francks, C., Baird, G., Conti-Ramsden, G., Clark, A., et al. (2015). Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'. EUROPEAN JOURNAL OF HUMAN GENETICS, 23(9), 1113-1115 [10.1038/ejhg.2014.275].
Ceroni, Fabiola; Simpson, Nuala H.; Francks, Clyde; Baird, Gillian; Conti-Ramsden, Gina; Clark, Ann; Bolton, Patrick F.; Hennessy, Elizabeth R.; Donne...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/525630
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